Methods and kits for providing lift and then a permanent color to hair

ABSTRACT

Disclosed are methods and kits for coloring the hair involving a lifting composition capable of lightening the natural hair color, a color base composition comprising at least one primary dye intermediate, and a developer composition comprising an oxidizing agent chosen from persulfates, perborates, percarbonates, and mixtures thereof.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a National Phase filing under 35 U.S.C. §371 of PCT/IB2009/007034 filed on Aug. 28, 2009; and this application claims priority to U.S. Provisional Application No. 61/092,770 filed on Aug. 29, 2008 under 35 U.S.C. §119; the entire contents of all are hereby incorporated by reference.

BACKGROUND OF THE INVENTION

Imparting a color change or color effect on hair can be done using permanent and semi-permanent or temporary hair coloring products. Conventional permanent hair coloring products are dye compositions comprising oxidation dye precursors, which are also known as primary intermediates or couplers. These oxidation dye precursors are colorless or weakly colored compounds which, when combined with oxidizing products, give rise to colored complexes by a process of oxidative condensation. The oxidizing products conventionally use peroxides such as hydrogen peroxide as oxidizing agents. Such permanent hair color products also contain ammonia or other alkalizing agents such as monoethanolamine (MEA) which causes the hair shaft to swell, thus allowing the small oxidative dye molecules to penetrate the cuticle and cortex before the oxidation condensation process is completed. The resulting larger-sized colored complexes from the oxidative reaction are then trapped inside the hair fiber, thereby permanently altering the color of the hair.

It is also known that it is possible to vary the shades obtained with the primary intermediates by combining them with couplers or coloration modifiers. The variety of molecules used as primary intermediates and couplers can allow a wide range of colors to be obtained.

The artificial color of hair treated with a permanent hair coloring product does not easily wash out during the course of routine shampooing. The colorations obtained show good longevity (also referred to as color-fastness) with exposure to shampoo.

It is desirable to many consumers to have the ability to lift the color of their hair whenever desired during the process of coloring their hair. Lifting is defined as the process by which the natural hair melanin is removed, thereby leaving the hair lightened from its natural color. During the lifting process, the alkaline environment ensures that the cuticles of the hair are opened to allow penetration of an oxidizing agent, such as hydrogen peroxide. Such an oxidizing agent breaks down the melanin by providing it with oxygen, and the melanin molecule is colorless when oxidized.

It has been surprisingly found that a desirable lift and color on hair can be achieved by employing the steps of applying a lifting composition capable of lightening the natural hair color, followed by a color base composition containing at least one primary dye intermediate, and then followed by application of a developer composition containing at least one oxidizing agent chosen from persulfates, perborates, percarbonates, and salts thereof, either immediately after, or at any time thereafter that is convenient to the consumer from the time of application of the color base composition, for example up to 60 minutes thereafter. By using this method, the following several significant advantages can be realized, as compared to the use of conventional permanent dyeing techniques: a desirable lightening of natural hair color; shorter dyeing time; comparable color-fastness to conventional permanent hair dyeing methods using peroxide developers; improved color deposit on the hair; little to no odor. In some instances, depending on the oxidative dye and/or coupler molecule used, different colors/shades may be obtained compared to the conventional hair coloring compositions/methods using peroxide developers.

Another disadvantage associated with the use of conventional permanent hair dye formulations and systems is that they are very messy to apply and have a tendency to cause scalp staining.

Thus, it is also an object of the present invention to provide a means of permanently coloring hair in a less messy or cleaner manner, while at the same time, provide a desirable lift to or lightening of the hair color.

Another object of the present invention is to provide a means of permanently coloring hair in the absence of peroxide raw material ingredient.

BRIEF SUMMARY OF THE INVENTION

The present invention is directed to a method of permanently coloring hair involving the steps of:

(a) applying onto the hair a lifting composition capable of lightening the natural hair color;

(b) rinsing the lifting composition from the hair;

(c) providing a color base composition containing at least one primary dye intermediate chosen from ortho-aminophenols, para-aminophenols, ortho-phenylenediamines, para-phenylenediamines, double bases, heterocyclic bases, the acid addition salts thereof, and mixtures thereof; (d) applying the color base composition onto the hair; (e) rinsing the color base composition from the hair; (f) providing a developer composition containing at least one oxidizing agent chosen from persulfates, perborates, percarbonates, their salts, and mixtures thereof; and (g) applying the developer composition onto the hair in order to develop color, in situ, in the hair to form colored hair; and (h) rinsing the developer composition from the hair.

According to a preferred embodiment, the color base composition and the developer composition are each substantially free of any oxidation catalyst. By “substantially free”, it is meant that the color base composition does not contain more than 0.2% by weight of oxidation catalyst, preferably not more than 0.1% by weight. According to a particularly preferred embodiment, the color base composition does not contain any oxidation catalyst. Similarly, according to a preferred embodiment, the color base composition and the developer composition are each free of peroxide, that is to say, they do not contain peroxide

The present invention is also directed to a kit for permanently coloring hair, the kit containing:

(a) a multi-unit receptacle;

(b) at least one unit comprising a lifting composition capable of lightening the natural hair color;

(c) at least one unit comprising a color base composition containing at least one primary dye intermediate chosen from ortho-aminophenols, para-aminophenols, ortho-phenylenediamines, para-phenylenediamines, double bases, heterocyclic bases, the acid addition salts thereof, and mixtures thereof; and (d) at least one unit comprising a developer composition containing at least one oxidizing agent chosen from persulfates, perborates, percarbonates, their salts, and mixtures thereof.

Here, too, according to a preferred embodiment, the color base composition and the developer composition are each substantially free of any oxidation catalyst.

Similarly, according to a preferred embodiment, the color base composition and the developer composition are each free of peroxide.

It should be noted that by varying the pH of the system, different levels of color vibrancy can be achieved.

DETAILED DESCRIPTION OF THE INVENTION

Other than in the operating examples, or where otherwise indicated, all numbers expressing quantities of ingredients or reaction conditions are to be understood as being modified in all instances by the term “about”.

As used herein, the expression “at least one” means one or more and thus includes individual components as well as mixtures/combinations.

As used herein, the term “applying” means contacting the hair to be dyed with the dye composition or with at least one of the compositions of the invention.

As used herein, “cosmetically acceptable” means that the item in question is compatible with any human keratin material and in particular human keratinous fibers, such as human hair.

As used herein, “natural hair color” refers to the color of hair resulting from the melanin pigments present in the hair.

As used herein, “conditioning” means imparting to at least one keratinous fiber at least one property chosen from combability, manageability, moisture-retentivity, luster, shine, and softness. In case of combing, the level of conditioning is evaluated by measuring, and comparing, the ease of combability of the treated hair and of the untreated hair in terms of combing work (gm-in).

As used herein, “formed from,” means obtained from chemical reaction of, wherein “chemical reaction,” includes spontaneous chemical reactions and induced chemical reactions. As used herein, the phrase “formed from”, is open ended and does not limit the components of the composition to those listed, e.g., as component (i) and component (ii). Furthermore, the phrase “formed from” does not limit the order of adding components to the composition or require that the listed components (e.g., components (i) and (ii)) be added to the composition before any other components.

As used herein, the term “rheology modifier” means any compound capable of giving a viscosity to the oxidizing composition such that, once it is applied onto keratin fibres, this composition does not run, and remains perfectly localized at the point of application.

1. Lifting Composition

The present invention involves the use of a lifting composition, which must be applied to the hair prior to application of the color base composition.

Any conventional lifting composition capable of removing color from or lightening the natural color of hair can be used in the present invention.

According to a preferred embodiment, the lifting composition comprises at least one oxidizing agent, chosen from the group formed by hydrogen peroxide, urea peroxide, alkali metal bromates, alkali metal ferricyanides, and persalts, such as perborates and persulphates. Use may also be made, as oxidizing agent, of one or more oxidation-reduction enzymes, such as laccases, peroxidases and 2-electron oxidoreductases (such as uricase), optionally in the presence of their respective donor or cofactor.

The use of hydrogen peroxide as oxidizing agent is preferred. Therefore, according to a particularly preferred embodiment, the lifting composition is an aqueous solution comprising hydrogen peroxide, the content of which can vary, more particularly, from about 1 to 40 volumes and more preferably still from about 5 to 40 volumes.

Various degrees of lift or lightening are achieved by varying the concentrations of the oxidizing agent in the lifting composition. For example, by using a lifting composition with a higher concentration of the oxidizing agent, a dark brown color may be lifted to a light brown as opposed to using a lifting composition with less of the oxidizing agent to achieve a medium brown color. The various degrees of lift may also be referred to as “levels” in number designations; the higher the level number, the more lift is achieved.

Depending on the desired aesthetic look, one of ordinary skill of the art will be able to determine which specific type of lifting composition to employ in order to achieve the desired degree of lift.

The lifting composition may also contain an alkalizing agent such as ammonia, alkaline carbonates, alkanolamines, such as mono-, di- and triethanolamines, and their derivatives, hydroxyalkylamines and ethylenediamines which are oxyethylenated and/or oxypropylenated, sodium hydroxide, potassium hydroxide and the compounds of the following formula:

in which R is a propylene residue optionally substituted by a hydroxyl group or a C₁-C₄ alkyl radical and R₂₂, R₂₃, R₂₄ and R₂₅, which are identical or different, represent a hydrogen atom, a C₁-C₄ alkyl radical or a C₁-C₄ hydroxyalkyl radical.

As alkalizing agent, ammonia is particularly preferred.

Examples of commercially available lifting compositions which may be used in accordance with the present invention include but are not limited to L'Oréal Excellence Crème Lights Highlighting kit, L'Oréal Quick Blue, Clairol BW2, L'Oréal Super Oreal Bleach, Miss Clairol Luminize Clear, Matrix V-Light, Logics Light Reactions, Redken Levitation, Feria 200, and Feria 205.

2. Color Base Composition

The present invention also involves the use of a color base composition, containing at least one primary dye intermediate.

In this invention, the color base composition may contain a wide variety of oxidation dye precursors. These include one or more primary dye intermediates and, optionally, one or more couplers.

A. Primary Dye Intermediates

Suitable primary dye intermediates are well known for use in hair color, and include ortho or para aminophenols, ortho or para phenylenediamines, double bases, heterocyclic bases, and the acid addition salts thereof.

The para-phenylenediamines, which can be used as primary dye intermediates in the color base composition of the invention, can be chosen in particular from the compounds of the following formula (I) and their addition salts with an acid:

in which: R₈ represents a hydrogen atom, a C₁-C₄ alkyl radical, a C₁-C₄ monohydroxyalkyl radical, a C₂-C₄ polyhydroxyalkyl radical, a (C₁-C₄)alkoxy(C₁-C₄)alkyl radical, a C₁-C₄ alkyl radical substituted by a nitrogenous group, a phenyl radical or a 4′-aminophenyl radical; R₉ represents a hydrogen atom, a C₁-C₄ alkyl radical, a C₁-C₄ monohydroxyalkyl radical, a C₂-C₄ polyhydroxyalkyl radical, a (C₁-C₄)alkoxy(C₁-C₄)alkyl radical or a C₁-C₄ radical substituted by a nitrogenous group; R₈ and R₉ can also form, with the nitrogen atom which carries them, a 5- or 6-membered nitrogenous heterocycle optionally substituted by one or more alkyl, hydroxyl or ureido groups; R₁₀ represents a hydrogen atom, a halogen atom, such as a chlorine atom, a C₁-C₄ alkyl radical, a sulpho radical, a carboxyl radical, a C₁-C₄ monohydroxyalkyl radical, a C₁-C₄ hydroxyalkoxy radical, a C₁-C₄ acetylaminoalkoxy radical, a C₁-C₄ mesylaminoalkoxy radical or C₁-C₄ carbamoylaminoalkoxy radicals; R₁₁ represents a hydrogen atom, a halogen atom or a C₁-C₄ alkyl radical.

Mention may in particular be made, among the nitrogenous groups in the above formula (I), of the amino, mono(C₁-C₄)alkylamino, di(C₁-C₄)alkylamino, tri(C₁-C₄)alkylamino, monohydroxy(C₁-C₄)alkylamino, imidazolinium and ammonium radicals.

Mention may more particularly be made, among the para-phenylenediamines of above formula (I), of para-phenylenediamine, para-toluoylenediamine, 2-chloro-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,5-dimethyl-para-phenylenediamine, N,N-dimethyl-para-phenylenediamine, N,N-diethyl-para-phenylenediamine, N,N-dipropyl-para-phenylenediamine, 4-amino-N,N-diethyl-3-methylaniline, N,N-bis(β-hydroxyethyl)-para-phenylenediamine, 4-N,N-bis(β-hydroxyethyl)amino-2-methylaniline, 4-N,N-bis(β-hydroxyethyl)amino-2-chloroaniline, 2-(β-hydroxyethyl)-para-phenylenediamine, 2-fluoro-para-phenylenediamine, 2-isopropyl-para-phenylenediamine, N-(β-hydroxypropyl)-para-phenylenediamine, 2-hydroxymethyl-para-phenylenediamine, N,N-dimethyl-3-methyl-para-phenylenediamine, N-ethyl-N-(β-hydroxyethyl)-para-phenylenediamine, N-(β,γ-dihydroxypropyl)-para-phenylenediamine, N-(4′-aminophenyl)-para-phenylenediamine, N-phenyl-para-phenylenediamine, 2-(β-hydroxyethyloxy)-para-phenylenediamine, 2-(β-acetylaminoethyloxy)-para-phenylenediamine, N-(β-methoxyethyl)-para-phenylenediamine, 2-methyl-1-N-(β-hydroxyethyl)-para-phenylenediamine and their addition salts with an acid.

Preference is very particularly given, among the para-phenylenediamines of above formula (I), to para-phenylenediamine, para-toluoylenediamine, 2-isopropyl-para-phenylenediamine, 2-(β-hydroxyethyl)-para-phenylenediamine, 2-(β-hydroxyethyloxy)-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, N,N-bis(β-hydroxyethyl)-para-phenylenediamine, 2-chloro-para-phenylenediamine and their addition salts with an acid.

Among the ortho-phenylenediamines, mention may be made of N1-(2-hydroxyethyl)-4-nitro-o-phenylenediamine, 4-methyl-o-phenylenediamine, and 4-nitro-o-phenylenediamine and acid addition salts thereof.

As used herein, the term double bases means compounds comprising at least two aromatic nuclei having at least one of amino and hydroxyl groups.

Mention may in particular be made, among the double bases which can be used as primary dye intermediates in the color base composition in accordance with the invention, of the compounds corresponding to the following formula (II) and their addition salts with an acid:

in which:

-   -   Z₁ and Z₂, which are identical or different, represent a         hydroxyl or —NH, radical which can be substituted by a C₁-C₄         alkyl radical or by a connecting arm Y;     -   the connecting arm Y represents a linear or branched alkylene         chain comprising from 1 to 14 carbon atoms which can be         interrupted or terminated by one or more nitrogenous groups         and/or by one or more heteroatoms, such as oxygen, sulphur or         nitrogen atoms, and which is optionally substituted by one or         more hydroxyl or C₁-C₆ alkoxy radicals;     -   R₁₂ and R₁₃ represent a hydrogen or halogen atom, a C₁-C₄ alkyl         radical, a C₁-C₄ monohydroxyalkyl radical, a C₂-C₄         polyhydroxyalkyl radical, a C₁-C₄ aminoalkyl radical or a         connecting arm Y;     -   R₁₄, R₁₅, R₁₆, R₁₇, R₁₈ and R₁₉, which are identical or         different, represent a hydrogen atom, a connecting arm Y or a         C₁-C₄ alkyl radical;         it being understood that the compounds of formula (II) only         comprise a single connecting arm Y per molecule.

Mention may in particular be made, among the nitrogenous groups of the above formula (II), of the amino, mono(C₁-C₄)alkylamino, di(C₁-C₄)alkyl amino, tri(C₁-C₄)alkylamino, monohydroxy(C₁-C₄)alkyl amino, imidazolinium and ammonium radicals.

Mention may more particularly be made, among the double bases of above formula (II), of N,N′-bis(β-hydroxyethyl)-N,N′-bis(4′-aminophenyl)-1,3-diamino-propanol, N,N′-bis(β-hydroxyethyl)-N,N′-bis(4′-aminophenyl)ethylenediamine, N,N′-bis(4-aminophenyl)-tetramethylenediamine, N,N′-bis(β-hydroxyethyl)-N,N′-bis(4-aminophenyl)tetramethylenediamine, N,N′-bis(4-methylaminophenyl)tetramethylenediamine, N,N′-diethyl-N,N′-bis(4′-amino-3′-methylphenyl)ethylenediamine, 1,8-bis(2,5-diaminophenoxy)-3,5-dioxaoctane and their addition salts with an acid. N,N′-Bis(β-hydroxyethyl)-N,N′-bis(4′-aminophenyl)-1,3-diaminopropanol, 1,8-bis(2,5-diaminophenoxy)-3,5-dioxaoctane or one of their addition salts with an acid are particularly preferred among these double bases of formula (II).

The para-aminophenols which can be used in the context of the invention can be chosen in particular from the compounds corresponding to the following formula (III) and their addition salts with an acid:

in which:

-   -   R₂₀ represents a hydrogen atom, a halogen atom, such as         fluorine, a C₁-C₄ alkyl radical, a C₁-C₄ monohydroxyalkyl         radical, a (C₁-C₄)alkoxy(C₁-C₄)alkyl radical, a C₁-C₄ aminoalkyl         radical or a hydroxy(C₁-C₄)alkylamino-(C₁-C₄)alkyl radical,     -   R₂₁ represents a hydrogen atom, a halogen atom, such as         fluorine, a C₁-C₄ alkyl radical, a C₁-C₄ monohydroxyalkyl         radical, a C₂-C₄ polyhydroxyalkyl radical, a C₁-C₄ aminoalkyl         radical, a C₁-C₄ cyanoalkyl radical or a         (C₁-C₄)alkoxy(C₁-C₄)alkyl radical.

Among the preferred para-aminophenols, mention may be made of para-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 4-amino-3-hydroxymethylphenol, 4-amino-2-methylphenol, 4-amino-2-hydroxymethyl phenol, 4-amino-2-methoxymethylphenol, 4-amino-2-aminomethylphenol, 4-amino-2-(3-hydroxyethylaminomethyl)phenol, N-methyl-para-aminophenol, and the acid addition salts thereof.

The ortho-aminophenols that may be used as primary dye intermediates in the context of the present invention may be chosen from 2-aminophenol, 2-amino-1-hydroxy-5-methylbenzene, 2-amino-1-hydroxy-6-methylbenzene, 5-acetamido-2-aminophenol, and the acid addition salts thereof.

Among the heterocyclic bases that can be used as primary dye intermediates in the color base composition of the present invention, mention may be made of pyridine derivatives, pyrimidine derivatives, pyrazole derivatives, pyrazolinone derivatives, and the acid addition salts thereof.

Among the pyridine derivatives, mention may be made of the compounds described, for example, in patents GB 1,026,978 and GB 1,153,196, such as 2,5-diaminopyridine, 2-(4-methoxyphenyl)amino-3-aminopyridine, 2,3-diamino-6-methoxypyridine, 2-(β-methoxyethyl)amino-3-amino-6 methoxypyridine, 3,4-diaminopyridine, and the acid addition salts thereof.

Among the pyrimidine derivatives, mention may be made of the compounds disclosed, for example, in German Patent DE 2 359 399 or Japanese Patents JP 88-169 571 and JP 91-10659 or Patent Application WO 96/15765, such as 2,4,5,6-tetra-aminopyrimidine, 4-hydroxy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triamino-pyrimidine, 2,4-dihydroxy-5,6-diaminopyrimidine, 2,5,6-triaminopyrimidine, and the pyrazolopyrimidine derivatives, such as those mentioned in French Application FR-A-2 750 048 and among which may be mentioned pyrazolo[1,5-a]pyrimidine-3,7-diamine; 2,5-dimethylpyrazolo[1,5-a]pyrimidine-3,7-diamine; pyrazolo[1,5-a]pyrimidine-3,5-diamine; 2,7-dimethylpyrazolo[1,5-a]pyrimidine-3,5-diamine; 3-aminopyrazolo[1,5-a]pyrimidin-7-ol; 3-aminopyrazolo[1,5-a]pyrimidin-5-ol; 2-(3-aminopyrazolo[1,5-a]pyrimidin-7-ylamino)ethanol; 2-(7-aminopyrazolo[1,5-a]pyrimidin-3-ylamino)ethanol; 2-[(3-aminopyrazolo[1,5-a]pyrimidin-7-yl)(2-hydroxyethyl)amino]ethanol; 2-[(7-aminopyrazolo[1,5-a]pyrimidin-3-yl)(2-hydroxyethyl)amino]ethanol; 5,6-dimethyl-pyrazolo[1,5-a]pyrimidine-3,7-diamine; 2,6-dimethylpyrazolo[1,5-a]pyrimidine-3,7-diamine; 2,5,N7,N7-tetramethylpyrazolo[1,5-a]pyrimidine-3,7-diamine; 3-amino-5-methyl-7-(imidazolylpropylamino)pyrazolo[1,5-a]pyrimidine; and their addition salts and their tautomeric forms, when there exists a tautomeric equilibrium, and their addition salts with an acid.

Among the pyrazole and pyrazolinone derivatives, mention may be made the compounds described in patents DE 3,843,892, DE 4,133,957 and patent applications WO 94/08969, WO 94/08970, FR-A-2,733,749, and DE 195 43 988, such as 4,5-diamino-1-methyl-pyrazole, 3,4-diaminopyrazole, 4,5-diamino-1-(4′-chlorobenzyl)pyrazole, 4,5-diamino-1,3-dimethylpyrazole, 4,5-diamino-3-methyl-1-phenylpyrazole, 4,5-diamino-1-methyl-3-phenylpyrazole, 4-amino-1,3-dimethyl-5-hydrazinopyrazole, 1-benzyl-4,5-diamino-3-methylpyrazole, 4,5-diamino-3-tert-butyl-1-methylpyrazole, 4,5-diamino-1-tert-butyl-3-methylpyrazole, 4,5-diamino-1-(β-hydroxyethyl)-3-methylpyrazole, 4,5-diamino-1-(β-hydroxyethyl)pyrazole, 4,5-diamino-1-ethyl-3-methylpyrazole, 4,5-diamino-1-ethyl-3-(4′-methoxyphenyl)pyrazole, 4,5-diamino-1-ethyl-3-hydroxymethylpyrazole, 4,5-diamino-3-hydroxymethyl-1-methylpyrazole, 4,5-diamino-3-hydroxymethyl-1-isopropylpyrazole, 4,5-diamino-3-methyl-1-isopropylpyrazole, 4-amino-5-(2′-aminoethyl)amino-1,3-dimethyl-pyrazole, 3,4,5-triaminopyrazole, 1-methyl-3,4,5-triaminopyrazole, 3,5-diamino-1-methyl-4-methylaminopyrazole, 3,5-diamino-4-(β-hydroxyethyl)amino-1-methylpyrazole, 2-(4,5-diamino-1H-pyrazol-1-yl), H₂SO₄, 2,3-diamino-6,7-dihydro-1H,5H-pyrazolo[1,2-z]pyrazol-1-one, 1-methyl-3-phenyl-2-pyrazolinone, and the acid addition salts thereof.

Preferred primary dye intermediates are p-phenylenediamine, p-aminophenol, o-aminophenol, N,N-bis(β-hydroxyethyl)-p-phenylenediamine, 2,5-diaminotoluene, their salts and mixtures thereof.

The primary dye intermediates may be employed in amounts ranging from 0.0001% to 12% by weight, preferably from 0.0001% to 8.0% by weight, more preferably, from 0.005% to 5% by weight, based on the total weight of the color base composition.

B. Color Couplers

The color base composition of the present invention may also contain one or more coupler compounds. The couplers that may be used in the dyeing method disclosed herein include those conventionally used in oxidation dye compositions, that is to say, meta-aminophenols, meta-phenylenediamines and meta-diphenols, naphthols, mono- or polyhydroxylated naphthalene derivatives, and heterocyclic couplers such as, for example, indole derivatives, indoline derivatives, sesamol and its derivatives, pyridine derivatives, pyrazolotriazole derivatives, pyrazolones, indazoles, benzimidazoles, benzothiazoles, benzoxazoles, 1,3-benzodioxoles, quinolines, benzomorpholine derivatives, pyrazoloazole derivatives, pyrroloazole derivatives, imidazoloazole derivatives, pyrazolopyrimidine derivatives, pyrazoline-3,5-dione derivatives, pyrrolo[3,2-d]oxazole derivatives, pyrazolo[3,4-d]thiazole derivatives, thiazoloazole S-oxide derivatives, thiazoloazole S,S-dioxide derivatives, and the acid addition salts thereof.

Suitable color couplers include, for example, those having the general formula (IV):

wherein R₁ is unsubstituted hydroxy or amino, or hydroxy or amino substituted with one or more C₁₋₆ hydroxyalkyl groups, R₃ and R₅ are each independently hydrogen, hydroxy, amino, or amino substituted with C₁₋₆ alkyl, C₁₋₆ alkoxy, or C₁₋₆ hydroxyalkyl group; and R₂, R₄, and R₆ are each independently hydrogen, C₁₋₆ alkoxy, C₁₋₆ hydroxyalkyl, or C₁₋₆ alkyl, or R₃ and R₄ together may form a methylenedioxy or ethylenedioxy group. Examples of such compounds include meta-derivatives such as phenols, meta-aminophenols, meta-phenylenediamines, and the like, which may be unsubstituted, or substituted on the amino group or benzene ring with alkyl, hydroxyalkyl, alkylamino groups, and the like. Suitable couplers include m-aminophenol, 2,4-diaminotoluene, 4-amino, 2-hydroxytoluene, phenyl methyl pyrazolone, 3,4-methylenedioxyphenol, 3,4-methylenedioxy-1-[(beta-hydroxyethyl)amino]benzene, 1-methoxy-2-amino-4-[(beta-hydroxyethyl)amino]benzene, 1-hydroxy-3-(dimethylamino)benzene, 6-methyl-1-hydroxy-3[(beta-hydroxyethyl)amino]benzene, 2,4-dichloro-1-hydroxy-3-aminobenzene, 1-hydroxy-3-(diethylamino)benzene, 1-hydroxy-2-methyl-3-aminobenzene, 2-chloro-6-methyl-1-hydroxy-3-aminobenzene, 1,3-diaminobenzene, 6-methoxy-1,3-diaminobenzene, 6-hydroxyethoxy-1,3-diaminobenzene, 6-methoxy-5-ethyl-1,3-diaminobenzene, 6-ethoxy-1,3-diaminobenzene, 1-bis(beta-hydroxyethyl)amino-3-aminobenzene, 2-methyl-1,3-diaminobenzene, 6-methoxy-1-amino-3-[(beta-hydroxyethyl)amino]-benzene, 6-(beta-aminoethoxy)-1,3-diaminobenzene, 6-(beta-hydroxyethoxy)-1-amino-3-(methylamino)benzene, 6-carboxymethoxy-1,3-diaminobenzene, 6-ethoxy-1-bis(beta-hydroxyethyl)amino-3-aminobenzene, 6-hydroxyethyl-1,3-diaminobenzene, 1-hydroxy-2-isopropyl-5-methylbenzene, 1,3-dihydroxybenzene, 2-chloro-1,3-dihydroxybenzene, 2-methyl-1,3-dihydroxybenzene, 4-chloro-1,3-dihydroxybenzene, 5,6-dichloro-2-methyl-1,3-dihydroxybenzene, 1-hydroxy-3-amino-benzene, 1-hydroxy-3-(carbamoylmethylamino)benzene, 6-hydroxybenzomorpholine, 4-methyl-2,6-dihydroxypyridine, 2,6-dihydroxypyridine, 2,6-diaminopyridine, 6-aminobenzomorpholine, 1-phenyl-3-methyl-5-pyrazolone, 1-hydroxynaphthalene, 1,7-dihydroxynaphthalene, 1,5-dihydroxynaphthalene, 5-amino-2-methyl phenol, 4-hydroxyindole, 4-hydroxyindoline, 6-hydroxyindole, 6-hydroxyindoline, 2,4-diamionphenoxyethanol, and mixtures thereof.

Other couplers may be chosen, for example, from 2,4-diamino-1-(β-hydroxyethyloxy)benzene, 2-methyl-5-aminophenol, 5-N-(β-hydroxyethyl)amino-2-methylphenol, 3-aminophenol, 1,3-dihydroxybenzene, 1,3-dihydroxy-2-methylbenzene, 4-chloro-1,3-dihydroxybenzene, 2,4-diamino 1-(β-hydroxyethyloxy)benzene, 2-amino-4-(β-hydroxyethylamino)-1-methoxybenzene, 1,3-diaminobenzene, 1,3-bis(2,4-diaminophenoxy)propane, sesamol, 1-amino-2-methoxy-4,5-methylenedioxybenzene, α-naphthol, 6-hydroxyindole, 4-hydroxyindole, 4-hydroxy-N-methylindole, 6-hydroxyindoline, 2,6-dihydroxy-4-methylpyridine, 1H-3-methylpyrazol-5-one, 1-phenyl-3-methylpyrazol-5-one, 2-amino-3-hydroxypyridine, 3,6-dimethylpyrazolo[3,2-c]-1,2,4-triazole, 6-dimethylpyrazolo[1,5-b]-1,2,4-triazole, 6-methylpyrazolo[1,5-a]-benzimidazole, and the acid addition salts thereof.

Preferred couplers include resorcinol, 1-naphthol, 2-methylresorcinol, 4-amino-2-hydroxy toluene, m-aminophenol, 2,4-diaminophenoxyethanol, phenyl methylpyrazolone, hydroxybenzomorpholine, 2-methyl-5-hydroxyetyylaminophenol, 6-hydroxyindole, 2-amino-3-hydroxypyridine, 5-amino-6-chloro-o-cresol, 4-chlororesorcinol, their salts, and mixtures thereof.

When they are present, these couplers may be present in amounts ranging from 0.00010 to 12% by weight; preferably from 0.001% to 8% by weight, based on the total weight of the color base composition.

In general, the acid addition salts of the oxidation bases and couplers may be chosen from hydrochlorides, hydrobromides, sulphates, tartrates, lactates, and acetates.

C. Cosmetically Acceptable Medium

The color base composition of the invention is generally formulated in a cosmetically acceptable medium, which can comprise at least one solvent chosen from water, organic solvents and mixtures thereof.

Preferably, the color base composition of the present invention comprises at least 5% by weight, more preferably at least 20% by weight, and even more preferably at least 30% by weight of water, based on the total weight of said color base composition.

According to a preferred embodiment, the color base composition comprises water and at least one co-solvent chosen from organic solvents.

Suitable organic solvents include alcohols, such as ethanol, isopropyl alcohol, benzyl alcohol and phenyl ethyl alcohol; glycols and glycol ethers, such as ethylene glycol, propylene glycol, hexylene glycol, ethylene glycol monomethyl, monoethyl or monobutyl ether, propylene glycol and its ethers, such as propylene glycol monomethyl ether, butylene glycol, dipropylene glycol, and also diethylene glycol alkyl ethers, such as diethylene glycol monoethyl ether and monobutyl ether; hydrocarbons such as straight chain hydrocarbons, mineral oil, polybutene, hydrogenated polyisobutene, hydrogenated polydecene, polydecene, squalene, petrolatum and isoparaffins; and mixtures, thereof.

The at least one co-solvent may be present in an amount ranging from about 1% to about 30% by weight, such as from about 2% to about 20% by weight, relative to the total weight of the color base composition.

The color base composition of the present invention can be acidic, or alkaline.

Therefore, according to a first embodiment of the present invention, the color base composition has a pH ranging from 2 to 6.9, more preferably from 3 to 6.9, and even more preferably from 4.5 to 6.9.

According to a second embodiment of the present invention, the color base composition has a pH ranging from 7 to 12, more preferably from 8 to 11, and even more preferably from 9 to 10.

If necessary, suitable pH adjusters may be used to obtain the above-disclosed pH values. Examples of suitable pH adjusters include, but are not limited to, monoethanolamine, ammonium hydroxide, sodium hydroxide, arginine, aminomethyl propanol.

D. Other Optional Ingredients of the Color Base Composition

The color base composition of the invention can also optionally contain other types of colorants. Suitable hair colorants include, but are not limited to, pigments, liposoluble dyes, direct dyes, nacreous pigments, pearling agents, leuco dyes, optical lightening colorants, natural colorants and optically-variable pigments.

Representative liposoluble dyes which may be used according to the present invention include Sudan Red, DC Red 17, DC Green 6, β-carotene, soybean oil, Sudan Brown, DC Yellow 11, DC Violet 2, DC Orange 5, DC Blue No. 14, annatto, and quinoline yellow. The liposoluble dyes, when present, may have a concentration ranging up to 20% by weight of the total weight of the color base composition, such as from 0.0001% to 6% by weight.

The nacreous pigments which may be used according to the present invention may be chosen from white nacreous pigments such as mica coated with titanium or with bismuth oxychloride, colored nacreous pigments such as titanium mica with iron oxides, titanium mica with ferric blue or chromium oxide, titanium mica with an organic pigment chosen from those mentioned above, and nacreous pigments based on bismuth oxychloride. The nacreous pigments, if present, may be present in the color base composition in a concentration ranging up to 50% by weight of the total weight of the color base composition, such as from 0.1% to 20% by weight, preferably from 0.1% to 15% by weight.

The pigments, which may be used according to the present invention, may be chosen from white, colored, inorganic, organic, polymeric, nonpolymeric, coated and uncoated pigments. Representative examples of mineral pigments include titanium dioxide, optionally surface-treated, zirconium oxide, zinc oxide, cerium oxide, iron oxides, chromium oxides, manganese violet, ultramarine blue, chromium hydrate, silica, ferric blue, and mixtures thereof. Representative examples of organic pigments include carbon black, pigments of D & C type, and lakes based on cochineal carmine, barium, strontium, calcium, and aluminum. Other examples of pigments are ultramarines, HC Blue No. 14, Ext. Yellow 7, Yellow 10 Lake, and acid violet 43.

If present, the pigments may be present in the color base composition in a concentration ranging up to 50% by weight of the total weight of the color base composition, such as from 0.5% to 40% by weight, and further such as from 2% to 30% by weight.

A direct dye is a colored substance that does not require the use of an oxidizing agent in order to reveal its color. Suitable direct dyes which may be used according to the present invention may be chosen from acidic (anionic), basic (cationic), and neutral dyes.

“Acidic dye” is generally intended to mean a dye containing at least one COON, SO₃H, PO_(S)H, or PO₄H₂ group, it being possible for said groups to exist in the form of salts. “Salts” is generally intended to mean salts of metals (for example, alkali metals or alkaline earth metals), salts of an organic amine that is optionally hydroxylated. Such dyes are also referred to as anionic dyes.

The acidic dyes that can be used in the context of this invention can be chosen from acidic nitro dyes, acidic azo dyes, acidic azine dyes, acidic triarylmethane dyes, acidic quinone dyes, acidic indo-amine dyes and acidic natural dyes, and mixtures thereof.

“Basic dyes” is generally intended to mean a dye that has at least one group bearing a positive charge, such as an ammonium group or a quaternized nitrogen atom in a ring. Such dyes are also referred to as cationic dyes.

The basic dyes that can be used in the context of this invention can be chosen from nitrobenzene dyes, azo dyes, azomethine dyes, methine dyes, tetraazapentamethine dyes, anthraquinone dyes, naphthoquinone dyes, benzoquinone dyes, phenothiazine dyes, indigoid dyes, xanthene dyes, phenanthridine dyes, phthalocyanin dyes, triarylamethane-derived dyes and basic natural dyes, and mixtures thereof.

Preferably, the direct dyes may be present in amounts ranging from 0.001% to 30% by weight, preferably from 0.01% to 20% by weight, more preferably from 0.1% to 10% by weight, based on the total weight of the color base composition.

Representative leuco dyes include those disclosed in US patent application publication no. 20040194231, the entire contents of which is hereby incorporated by reference. Leuco dyes are usually only slightly colored or are not colored at all and can be converted by simple oxidation in air or in the presence of an oxidizing agent into a triheteroylmethane compound. Examples of leuco dyes and corresponding triheteroylmethane compounds include 1H-Benzo[ij]quinolizinium, 9-[bis(2,3,6,7-tetrahydro-1H,5H-benzo[ij]quinolizin-9-yl)methylene]-2,3,5,6,7,9-hexahydro-chloride; 5H-Benzo[a]carbazolium, 11-ethyl-5-[(11-ethyl-11H-benzo[a]carbazol-5-yl)(1-ethyl-1,2,3,4-tetrahydro-5-quinolinyl)methylene]-; Pyrrolo[3,2,1-ij]quinolinium, 8-[bis(1,2,5,6-tetrahydro-4H-pyrrolo[-3,2,1-ij]quinolin-8-yl)methylene]-1,2,4,5,6,8-hexahydro-; Tri(9-ethyl-9H-carbazol-3-yl)methane; bis(6-Chloro-9-ethyl-9H-carbazol-3-yl)-(9-ethyl-9H-carbazol-3-yl)methane; bis(1-(4-sulfo-butyl)-2,3,4,6-tetrahydro-quinolinium)-pyrid-4-yl-methane; bis(1-ethyl-2-methyl-1H-indol-3-yl)-(9-ethyl-9H-carbazol-3-yl)methane; Tri(7-ethyl-7H-benzo[c]carbazol-10-yl)methane; bis((6-dimethylamino-3-methyl-1H-indol-2-yl)-2-furylmethane; bis((6-dimethylamino-3-methyl-1H-indol-2-yl)-(pyrid-4-yl)methane; bis(1-ethyl-2-methyl-1H-indol-3-yl)-2-thienylmethane; 3-[(1-ethyl-2-methyl-1H-indol-3-yl)-(9-ethyl-9H-carbazol-3-yl)methylene]-1-ethyl-2-methyl-3H-indolium; and 3-[(1-ethyl-2-methyl-1H-indol-3-yl)-2-thienyl)methylene]-1-ethyl-2-methyl-3H-indolium.

Representative optical lightening colorants include those disclosed in US patent application publication no. US20040205905, the entire contents of which is hereby incorporated by reference.

Representative natural colorants include those disclosed in US patent application publication no. US20030159221, the entire contents of which is hereby incorporated by reference. For the purposes of the invention, the expression “natural colorant” means compounds that exist in nature, whether they have been obtained by extraction or reproduced chemically. Examples of natural direct dyes that may be used according to the invention include lawsone, juglone, alizarin, purpurin, carminic acid, kermesic acid, purpurogallin, protocatechaldehyde, indigo, isatin, curcumin, spinulosin and apigenidin. It is also possible to use extracts or decoctions containing these natural dyes and especially henna-based poultices or extracts.

3. Developer Composition

The developer composition of the invention comprises, in a medium suitable for dyeing, at least one oxidizing agent present in an amount sufficient to develop a color. The oxidizing agent employed in this invention is selected from persulfates, perborates, percarbonates, their salts, and mixtures thereof.

Preferred persulfates are monopersulfates such as, for example, potassium persulfate, sodium persulfate, ammonium persulfate, as well as mixtures thereof.

The preferred oxidizing agents in the present invention are potassium persulfate, sodium persulfate and mixtures thereof.

The at least one oxidizing agent is present in an amount sufficient to generate color in the hair without destroying the oxidative dye precursors which have migrated into the hair prior to completion of the hair dyeing process to the desired color/shade.

In general, the at least one oxidizing agent will be present in an amount of at least 1% by weight, based on the total weight of the developer composition.

According to a preferred embodiment, the at least one oxidizing agent is present in an amount ranging from 1% by weight to 80% by weight, preferably from 5% to 75% by weight, more preferably from 6% to 10% by weight, based on the total weight of the developer composition.

Similarly, the developer composition is applied onto the hair for a period of time sufficient to generate color in the hair. In general, the developer composition is applied onto the hair for a period of from 1 to 20 minutes, such as from 1 to 10 minutes, for example from 1 to 5 minutes.

According to a first preferred embodiment of the invention, the developer composition is anhydrous.

The term “anhydrous” means that the developer composition is either completely free of water or contains no appreciable amount of water, preferably no more than 1% by weight, and more preferably no more than 0.5% by weight, based on the weight of the developer composition.

According to a particularly preferred embodiment of the invention, the developer composition is totally anhydrous, that is to say it does not contain any water.

The developer composition can contain at least one solvent, chosen from water, organic solvents, and mixtures thereof.

When the developer composition is substantially anhydrous or totally anhydrous, the at least one solvent is chosen from organic solvents.

Suitable organic solvents include ethanol, isopropyl alcohol, benzyl alcohol, phenyl ethyl alcohol, glycols and glycol ethers, such as ethylene glycol, propylene glycol, hexylene glycol, ethylene glycol monomethyl, monoethyl or monobutyl ether, propylene glycol and its ethers, such as propylene glycol monomethyl ether, butylene glycol, dipropylene glycol, diethylene glycol alkyl ethers, such as diethylene glycol monoethyl ether and monobutyl ether, hydrocarbons such as straight chain hydrocarbons, mineral oil, polybutene, hydrogenated polyisobutene, hydrogenated polydecene, polydecene, squalane, petrolatum, isoparaffins, and mixtures, thereof.

The at least one solvent may, for example, be present in an amount ranging from 0.5% to 70% by weight, such as from 2% to 60% by weight, preferably from 5 to 50% by weight, relative to the total weight of the developer composition.

The developer composition may be in the form of a powder, gel, liquid, foam, lotion, cream, mousse, and emulsion.

In a first preferred embodiment, the developer composition is in powder form.

In a second preferred embodiment, the developer composition is in the form of a gel.

According to another preferred embodiment, the developer composition may be formed right before use by combining an anhydrous oxidizer composition containing at least one oxidizing agent chosen from persulfates, perborates, percarbonates, their salts, and mixtures thereof, and a shampoo composition containing at least one surfactant.

The at least one surfactant in the shampoo composition can be chosen from anionic, amphoteric, nonionic, zwitterionic, cationic surfactants, and mixtures thereof.

It should be noted that the use of a catalyst during the oxidation of the oxidative dye precursor such as, for example, cupric or ferrous salt, is not necessary in order to achieve a desired color/shade.

Thus, according to a preferred embodiment of the present invention, the lifting composition, the color base composition, and the developer composition of the present invention are substantially free of an oxidation catalyst, i.e., such catalyst is present in a less than catalytically effective amount in the lifting, color base, and developer compositions.

As used herein, “oxidation catalyst” refers to transition metal cations that can aid in the oxidation of certain dye precursors, such as cupric and ferrous ions.

According to a particularly preferred embodiment, lifting composition, the color base composition, and the developer composition are each totally free of cupric ions and of ferrous ions.

According to another preferred embodiment, both the color base composition and the developer composition do not contain hydrogen peroxide (H₂O₂).

The pH of the developer composition can range from 3 to 11, such as from 6 to 11, and it may be adjusted to the desired value using basifying/alkalizing agents that are well known in the art in the dyeing of keratin fibers.

4. Additional Ingredients

The compositions used in the present invention may also include one or more additional ingredients, which may be incorporated into the color base composition, the developer composition, the lifting composition, or all three. Such ingredients include well-known conventional additives typically employed in hair coloring compositions such as basifying and acidifying agents, buffers, rheological modifiers, conditioning agents, surfactants, antioxidants, fragrances, and chelating agents.

A. Basifying Agents

Basifying (also called alkalizing) and acidifying agents may be used in the compositions of the present invention.

Examples of the basifying or alkalizing agents include ammonia, alcanolamines such as monoethanolamine, diethanolamine, triethanolamine, isopropanolamine, propane-1,3-diamine, oxyethylenated and oxypropylenated hydroxyalkylamines and ethylenediamines, polyamines, sodium hydroxide and potassium hydroxide, ammonium or alkali carbonates, ammonium or alkali bicarbonates, alkali metal carbonates, alkali silicates, alkali metasilicates, organic carbonates, alkali hydroxides, aminomethylpropanol, and mixtures thereof.

The basifying agents may, for example, be present in an amount ranging from 0.05% to 40% by weight, relative to the total weight of the composition of the present invention.

The basifying agents can also be used in the invention to adjust the pH of the lifting composition and/or the color base composition and/or the developer composition.

B. Rheological Modifiers

According to the invention, the lifting composition and/or the color base composition and/or the developer composition may also comprise at least one rheology modifier chosen from nonionic, anionic, cationic or amphoteric polymers, and other rheology modifiers such as cellulose-based thickeners (hydroxyethylcellulose, hydroxypropylcellulose, carboxymethylcellulose, cationic cellulose ether derivatives, quaternized cellulose derivatives, etc.), guar gum and its derivatives (hydroxypropyl guar, cationic guar derivatives, etc.), gums of microbial origin (xanthan gum, scleroglucan gum, etc.), crosslinked homopolymers of acrylic acid or of acrylamidopropanesulfonic acid and associative polymers as described below.

In particular, the compositions of the present invention may comprise at least one polymer chosen from nonionic, anionic, cationic or amphoteric amphiphilic polymers.

The amphiphilic polymers may contain a hydrophobic chain that is a saturated or unsaturated, aromatic or non-aromatic, linear or branched C₆-C₃₀ hydrocarbon-based chain, optionally comprising one or more oxyalkylene (oxyethylene and/or oxypropylene) units.

Among the cationic amphiphilic polymers comprising a hydrophobic chain that may be found are cationic polyurethanes or cationic copolymers comprising vinyllactam units and in particular vinylpyrrolidone units.

As examples of nonionic amphiphilic polymers containing a hydrophobic chain, mention may be made, inter alia, of:

(1) celluloses modified with groups comprising at least one saturated or unsaturated, linear or branched C₆-C₃₀ hydrocarbon-based chain, for instance hydroxyethylcelluloses modified with groups comprising at least one hydrophobic chain as defined previously, such as especially Natrosol Plus Grade 330 CS (C₁₆ alkyls—sold by the company Aqualon); Bermocoll EHM 100 (sold by the company Berol Nobel), Amercell Polymer HM-1500 (hydroxyethylcellulose modified with a polyethylene glycol (15) nonylphenyl ether group, sold by the company Amerchol);

(2) hydroxypropyl guars modified with groups comprising at least one hydrophobic chain as defined, for example Jaguar XC-95/3 (C₁₄ alkyl chain, sold by the company Rhodia Chimie); Esaflor HM 22 (C₂₂ alkyl chain—sold by the company Lamberti); RE210-18 (C₁₄ alkyl chain) and RE205-1 (C₂₀ alkyl chain) sold by the company Rhodia Chimie;

(3) copolymers of vinylpyrrolidone and of hydrophobic monomers containing a hydrophobic chain as defined above, for instance Antaron or Ganex V216 (vinylpyrrolidone/hexadecene copolymers); Antaron or Ganex V220 (vinylpyrrolidone/eicosene copolymers), sold by the company I.S.P.;

(4) copolymers of C₁-C₆ alkyl(meth)acrylates and of amphiphilic monomers containing a hydrophobic chain;

(5) copolymers of hydrophilic (meth)acrylates and of hydrophobic monomers comprising at least one hydrophobic chain, for instance the polyethylene glycol methacrylate/lauryl methacrylate copolymer;

(6) polymers with an aminoplast ether skeleton containing at least one fatty chain, such as the Pure Thix compounds sold by the company Sud-Chemie;

(7) linear (block structure), grafted or starburst polyurethane polyethers comprising in their chain at least one hydrophilic block, which is generally a polyoxyethylene block which may comprise between 50 and 1 000 oxyethylene units approximately, and at least one hydrophobic block, which may comprise aliphatic groups alone, optionally combined with cycloaliphatic and/or aromatic blocks. Preferably, the polyurethane polyethers comprise at least two C₆-C₃₀ hydrocarbon-based hydrophobic chains, separated by a hydrophilic block; the hydrophobic chains may be pendent chains or chains with one or more of the end groups of the hydrophilic block(s).

The polyurethane polyethers comprise a urethane bond between the hydrophilic blocks, but may also contain hydrophilic blocks linked to the lipophilic blocks via other chemical bonds.

Examples of polyurethane polyethers that may be mentioned include Nuvis FX 1100 (European and US INCI name “Steareth-100/PEG-136/HMDI Copolymer” sold by the company Servo Delden); Rheolate 205, 208, 204 or 212 (sold by the company Rheox); Elfacos T210 (C₁₂-C₁₄ alkyl chain) and Elfacos T212 (C₁₈ alkyl chain) sold by the company Akzo.

The anionic amphiphilic polymers containing a hydrophobic chain that may be used comprise, as hydrophobic chain, at least one saturated or unsaturated, aromatic or non-aromatic, linear or branched C₈-C₃₀ hydrocarbon-based chain.

More particularly, the anionic amphiphilic polymers comprising at least one hydrophobic chain which are crosslinked or non-crosslinked, comprise at least one hydrophilic unit derived from one or more ethylenically unsaturated monomers bearing a carboxylic acid function, or a sulphonic function which is free or partially or totally neutralized, and at least one hydrophobic unit derived from one or more ethylenically unsaturated monomers bearing a hydrophobic side chain, and optionally at least one crosslinking unit derived from one or more polyunsaturated monomers.

The anionic amphiphilic polymers may also comprise at least one sulphonic group, in free or partially or totally neutralized form and at least one hydrophobic portion.

Among these, mention may be made more particularly of acrylamido-2-methyl-2-propanesulphonic (AMPS) acid/n-dodecylacrylamide copolymer neutralized with sodium hydroxide, the copolymer crosslinked with methylenebisacrylamide consisting of 75% by weight of AMPS units neutralized by NH₃ and 25% by weight of Genapol T-250 acrylate units, the copolymer crosslinked with allyl methacrylate consisting of 90% by weight of AMPS units neutralized with NH₃ and 10% by weight of Genapol T-250 methacrylate units, or the copolymer crosslinked with allyl methacrylate consisting of 80% by weight of AMPS units neutralized with NH₃ and 20% by weight of Genapol T-250 methacrylate units.

Other examples include Carbopol ETD-2020 (acrylic acid/C₁₀-C₃₀ alkyl methacrylate crosslinked copolymer sold by the company Noveon); Carbopol 1382, Pemulen TR1 and Pemulen TR2 (acrylic acid/C₁₀-C₃₀ alkyl acrylate crosslinked copolymers—sold by the company Noveon), the methacrylic acid/ethyl acrylate/oxyethylenated stearyl methacrylate copolymer (55/35/10); the (meth)acrylic acid/ethyl acrylate/25 EO oxyethylenated behenyl methacrylate copolymer (Aculyn 28 sold by Rohm & Haas) and the methacrylic acid/ethyl acrylate/steareth-10 allyl ether crosslinked copolymer.

When one or more composition(s) of the present invention comprises one or more amphiphilic polymer(s) containing a hydrophobic chain, then this or these polymer(s) generally represent(s) from 0.01% to 20% by weight and preferably, from 0.05% to 10% by weight of the total weight of said composition(s).

The rheology modifier(s) that may be present in the compositions of the present invention can be chosen from polymers of natural origin or synthetic polymers, and are advantageously chosen from those conventionally used in cosmetics.

Examples of synthetic polymers that may be mentioned include polyvinylpyrrolidone, polyacrylic acid, polyacrylamide, non-crosslinked poly(2-acryl-amidopropanesulphonic acid) (Simugel EG from the company SEPPIC), crosslinked poly(2-acrylamido-2-methylpropanesulphonic acid), free or partially neutralized with ammonia (Hostacerin AMPS from Clariant), mixtures of non-crosslinked poly(2-acrylamido-2-methylpropanes-ulphonic acid) with hydroxyalkylcellulose ethers or with poly(ethylene oxide)s, as described in patent U.S. Pat. No. 4,540,510; mixtures of poly((meth)acrylamido(C₁-C₄)alkylsulphonic acid), which is preferably crosslinked, with a crosslinked copolymer of maleic anhydride and of a (C₁-C₅)alkyl vinyl ether (Hostacerin AMPS/Stabileze QM from the company ISF).

The thickening polymers of natural origin are preferably polymers comprising at least one sugar unit, for instance nonionic guar gums, optionally modified with C₁-C₆ hydroxyalkyl groups; biopolysaccharide gums of microbial origin, such as scleroglucan gum or xanthan gum; gums derived from plant exudates, such as gum arabic, ghatti gum, karaya gum, gum tragacanth, carrageenan gum, agar gum and carob gum; pectins; alginates; starches; hydroxy(C₁-C₆)alkylcelluloses and carboxy(C₁-C₆)alkylcelluloses.

It should be noted that the term “sugar unit” denotes a monosaccharide (i.e. monosaccharide or oside or simple sugar) portion, an oligosaccharide portion (short chains formed from a sequence of monosaccharide units, which may be different) or a polysaccharide portion [long chains consisting of monosaccharide units, which may be different, i.e. polyholosides or polyosides]. The saccharide units may also be substituted with alkyl, hydroxyalkyl, alkoxy, acyloxy or carboxyl radicals, the alkyl radicals containing from 1 to 4 carbon atoms.

Examples of nonionic, unmodified guar gums that may be mentioned, inter alia, include Guargel D/15 (Noveon); Vidogum GH 175 (Unipectine), Meypro-Guar 50 and Jaguar C (Meyhall/Rhodia Chimie); and the modified nonionic guar gums that may be mentioned include Jaguar HP8, HP60, HP120, DC 293 and HP 105 (Meyhall/Rhodia Chimie); Galactasol 4H4FD2 (Aqualon).

The biopolysaccharide gums of microbial or plant origin are well known to those skilled in the art and are described especially in the book by Robert L. Davidson entitled “Handbook of Water soluble gums and resins” published by McGraw Hill Book Company (1980).

Among these gums, mention will be made of scleroglucans such as, especially, Actigum CS from Sanofi Bio Industries; Amigel from Alban Muller International, and also the glyoxal-treated scleroglucans described in FR 2 633 940); xanthan gums, for instance Keltrol, Keltrol T, Keltrol Tf, Keltrol Bt, Keltrol Rd, Keltrol Cg (Nutrasweet Kelco), Rhodicare S and Rhodicare H (Rhodia Chimie); starch derivatives, for instance Primogel (Avebe); hydroxyethylcelluloses such as Cellosize QP3L, QP4400H, QP30000H, HEC30000A and Polymer PCG10 (Amerchol), Natrosol 250HHR, 250MR, 250M, 250HHXR, 250HHX, 250HR, HX (Hercules) and Tylose H1000 (Hoechst); hydroxypropylcelluloses, for instance Klucel EF, H, LHF, MF and G (Aqualon); carboxymethylcelluloses, for instance Blanose 7M8/SF, refined 7M, 7LF, 7MF, 9M31F, 12M31XP, 12M31P, 9M31XF, 7H, 7M31, 7H3SXF (Aqualon), Aquasorb A500 (Hercules), Ambergum 1221 (Hercules), Cellogen HP810A, HP6HS9 (Montello) and Primellose (Avebe).

When one or more composition(s) of the present invention comprises one or more rheology modifiers, then this or these rheology modifier(s) generally represent(s) from 0.01% to 20% by weight and better still from 0.05% to 10% by weight of the total weight of said composition(s).

C. Conditioning Agents

The lifting composition and/or the color base composition and/or the developer composition of the present invention may also contain at least one conditioning agent. Such conditioning agents are typically chosen from synthetic oils such as polyolefins, plant oils, fluoro oils or perfluoro oils, natural or synthetic waxes, silicones, non-polysaccharide cationic polymers, compounds of ceramide type, cationic surfactants, fatty amines, fatty acids and derivatives thereof, and also mixtures of these various compounds. Other useful conditioning agents are conditioning polymers which contain primary, secondary, tertiary and/or quaternary amine groups, forming part of the polymer chain or linked directly to the latter, and having a molecular weight of between 500 and approximately 5,000,000, and preferably between 1000 and 3,000,000.

Among these polymers, there may be mentioned, more especially, quaternized proteins, polymers of the polyamine, polyaminoamide or poly(quaternary ammonium) family and cationic polysiloxanes.

The quaternized proteins are, in particular, chemically modified polypeptides bearing quaternary ammonium groups at the end of the chain or grafted onto the latter.

Among the polyamine, polyaminoamide or poly(quaternary ammonium) family of polymers, there may be mentioned:

1) vinylpyrrolidone/dialkylaminoalkyl acrylate or methacrylate copolymers, quaternized or otherwise, such as the products sold by the company GAF CORPORATION under the name “GAFQUAT”, for example “GAFQUAT 734 or 755”, or alternatively the products designated “COPOLYMER 845, 958 and 937”. 2) The cellulose ether derivatives containing quaternary ammonium groups, especially the polymers marketed by the company UNION CARBIDE CORPORATION under the names “JR” (JR 400, JR 125, JR 30M) or “LR” (LR 400, LR 30M). The polymers are also defined in the CTFA Dictionary as quaternary ammonium derivatives of hydroxyethylcellulose subjected to reaction with an epoxide substituted with a trimethylammonium group. 3) Cationic cellulose derivatives such as cellulose copolymers or cellulose derivatives grafted with a water-soluble quaternary ammonium monomer such as, for example hydroxyalkylcelluloses such as hydroxymethyl-, hydroxyethyl- or hydroxypropylcellulose grafted with a methacryloylethyltrimethylammonium, methacrylamidopropyltrimethylammonium or dimethyldiallylammonium salt. Marketed products corresponding to this definition are, more especially, the products sold by the company NATIONAL STARCH under the names “CELQUAT L 200” and “CELQUAT H 100”. 4) The quaternized polysaccharides marketed under the name “JAGUAR C 13 S”, sold by the company MEYHALL. 5) Cyclopolymers having a molecular weight of 20,000 to 3,000,000 such as, for example, the homopolymer of dimethyldiallylammonium chloride sold by the company MERCK under the name “MERQUAT 100”, having a molecular weight of less than 100,000, and the copolymer of dimethyldiallylammonium chloride and acrylamide having a molecular weight above 500,000 and sold under the name “MERQUAT 550”. 6) Quaternary polymers of vinylpyrrolidone and of vinylimidazole, such as, for example, the products marketed by the company BASF under the names “LUVIQUAT FC 905, FC 550 and FC 370”.

Other conditioning polymers which are useable according to the invention are polyalkylenimines, especially polyethylenimines, polymers containing vinylpyridine or vinylpyridinium units, condensates of polyamines and epichlorohydrin, quaternary polyureylenes and chitin derivatives.

Other conditioning polymers which can be incorporated in the compositions of the invention are the cationic polysiloxanes such as those described in U.S. Pat. No. 4,185,087.

The conditioning polymers may also be chosen from amphoteric polymers, such as amphoteric polymers derived from chitosan or copolymers of diallyldialkylammonium and an anionic monomer.

Preferred polymers are, inter alia, polymers containing alkyl groups chosen from groups having 1 to 4 carbon atoms, and more especially methyl and ethyl groups.

Especially preferred conditioning polymers according to the invention are chosen from:

a) the poly(quaternary ammonium)polymers;

b) the copolymer of the diallyldimethylammonium chloride and acrylic acid (80/20) sold by the company CALGON under the name MERQUAT 280;

c) the homopolymer of dimethyldiallylammonium chloride sold by the company MERCK under the name MERQUAT 100;

d) the quaternized cellulose ether derivatives sold by the company UNION CARBIDE under the name JR;

e) the copolymer of vinylpyrrolidone and methacrylamidopropyltrimethylammonium chloride (85:15) sold by the company GAF under the name GAFQUAT HS100;

f) the polymeric quaternary ammonium salt of acrylamide and beta-methacrylyloxyethyl trimethyl ammonium methosulfate, sold by the company, Nalco, under the names polyquaternium-5 or quaternium-39 or Merquat 5; and

g) the cationic polymers of the ionene type sold by the company Chimex, such as hexadimethrine chloride, also known as IONENE G.

According to a preferred embodiment, the color base composition and the lifting composition both contain at least one conditioning agent as defined above. More preferably, the color base composition and the lifting composition each contains at least one conditioning polymer, in an amount of from 0.01% to 12% by weight, preferably from 0.1 to 10% by weight, more preferably from 0.1 to 8% by weight, all weights being based on the total weight of each composition.

D. Surfactants

The lifting composition and/or the color base composition and/or the developer composition may also contain at least one surfactant, chosen from anionic, amphoteric, non-ionic, zwitterionic, and cationic surfactants, and mixtures thereof.

The at least one surfactant may be chosen, for example, from the following:

(i). Anionic Surfactant(s):

The lifting composition and/or the color base composition and/or the developer composition may contain at least one anionic surfactant chosen, for example, from salts (for example, alkali metal salts, such as sodium salts, ammonium salts, amine salts, amino alcohol salts and magnesium salts) of the following compounds: alkyl sulphates, alkyl ether sulphates, alkylamino ether sulphates, alkylarylpolyether sulphates, monoglyceride sulphates; alkyl sulphonates, alkyl phosphates, alkyl amide sulphonates, alkyl aryl sulphonates, α-olefin sulphonates, paraffin sulphonates; (C₆-C₂₄)alkyl sulphosuccinates, (C₆-C₂₄)alkyl ether sulphosuccinates, (C₆-C₂₄)alkyl amide sulphosuccinates; (C₆-C₂₄)alkyl sulphoacetates; (C₆-C₂₄)acryl sarcosinates; and (C₆-C₂₄)acryl glutamates. At least one anionic surfactant may also be chosen, for example, from (C₆-C₂₄)alkylpolyglycoside carboxylic esters, such as alkylglucoside citrates, alkylpolyglycoside tartrates and alkylpolyglycoside sulphosuccinates, alkylsulphosuccinamates; acyl isethionates and N-acyl taurates, alkyl radicals and acyl radicals of these different compounds, such as those comprising from 12 to 20 carbon atoms, and at least one aryl radical may be chosen, for example, from phenyl and benzyl groups. At least one anionic surfactant may be chosen, for example, from fatty acid salts, such as oleic, ricinoleic, palmitic and stearic acid salts, coconut oil acid and hydrogenated coconut oil acid; acyl lactylates wherein the acyl radical comprises 8 to 20 carbon atoms. At least one anionic surfactant may be chosen, for example, from alkyl D-galactoside uronic acids and their salts, polyoxyalkylenated (C₆-C₂₄)alkyl ether carboxylic acids, polyoxyalkylenated (C₆-C₂₄)alkyl aryl ether carboxylic acids, polyoxyalkylenated (C₆-C₂₄)alkylamido ether carboxylic acids and their salts, for example, those comprising from 2 to 50 alkylene oxide groups, such as ethylene oxide groups, and mixtures thereof.

(ii) Non-Ionic Surfactant(s):

The lifting composition and/or the color base composition and/or the developer composition may contain at least one non-ionic surfactant chosen, for example, from non ionic surfactants compounds disclosed in “Handbook of Surfactants” by M. R. Porter, published by Blackie & Son (Glasgow and London), 1991, pp. 116-178. The at least one non-ionic surfactants may be chosen, for example, from polyethoxylated and/or polypropoxylated alkyl phenols, alpha-diols and alcohols, comprising fatty chains comprising, for example, from 8 to 18 carbon atoms, and the number of ethylene oxide and/or propylene oxide groups may range from 2 to 50. The at least one non-ionic surfactant may be chosen, for example, from copolymers of ethylene oxide and of propylene oxide, condensates of ethylene oxide and/or of propylene oxide with fatty alcohols; polyethoxylated fatty amides comprising, for example, from 2 to 30 mol of ethylene oxide, polyglycerolated fatty amides comprising on average 1 to 5, and, for example, 1.5 to 4, glycerol groups; polyethoxylated fatty amines comprising, for example, from 2 to 30 mol of ethylene oxide; oxyethylenated fatty acid esters of sorbitan comprising, for example, from 2 to 30 mol of ethylene oxide; fatty acid esters of sucrose, fatty acid esters of polyethylene glycol, alkylpolyglycosides, N-alkylglucamine derivatives, and amine oxides such as (C₁₀-C₁₄)alkyl amine oxides and N-acylaminopropylmorpholine oxides.

(iii) Amphoteric or Zwitterionic Surfactant(s):

The lifting composition and/or the color base composition and/or the developer composition may contain at least one amphoteric or zwitterionic surfactant that may be chosen, for example, from aliphatic secondary and tertiary amine derivatives wherein the aliphatic radical comprises linear and branched chains comprising 8 to 18 carbon atoms and comprising at least one water-solubilizing anionic group (for example, carboxylate, sulphonate, sulphate, phosphate and phosphonate); and (C₈-C₂₀)alkylbetaines, sulphobetaines, (C₈-C₂₀)alkylamido(C₁-C₆)alkylbetaines and (C₈-C₂₀)alkylamido(C₁-C₆)alkylsulphobetaines.

The at least one amine derivatives may be chosen, for example, from the products sold under the name Miranol, described in U.S. Pat. Nos. 2,528,378 and 2,781,354 and classified in the CTFA dictionary, 3rd edition, 1982, under the names Amphocarboxyglycinates and Amphocarboxypropionates, with the respective structures: R₂—CONHCH₂CH₂—N⁺(R₃)(R₄)(CH₂COO⁻)

wherein: R₂ is chosen from alkyl radicals of acids of formula R₂—COOH which are present in hydrolysed coconut oil, heptyl, nonyl and undecyl radicals; R₃ is chosen from beta-hydroxyethyl groups and R₄ is chosen from carboxymethyl groups; and R₂′—CONHCH₂CH₂—N(B)(C)

wherein:

B is chosen from —CH₂—CH₂—OX′; C is chosen from —(CH₂)_(z)—Y′, wherein z=1 or 2,

X′ is chosen from the —CH₂CH₂—COOH group and a hydrogen atom,

Y′ is chosen from —COOH and the —CH₂—CHOH—SO₃H radical,

R₂′ is chosen from alkyl radicals of acids R₉—COOH present in coconut oil and in hydrolysed linseed oil, alkyl radicals, such as C₇, C₉, C₁₁ and C₁₃ alkyl radicals, C₁₇ alkyl radicals and its is to form, and unsaturated C₁₇ radicals.

These compounds are classified, for example, in the CTFA dictionary, 5th edition, 1993, under the names Disodium Cocoamphodiacetate, Disodium Lauroamphodiacetate, Disodium Caprylamphodiacetate, Disodium Capryloamphodiacetate, Disodium Cocoamphodipropionate, Disodium Lauroamphopropionate, Disodium Caprylamphodipropionate, Disodium Caprylamphodipropionate, Lauroamphodipropionic acid and Cocoamphodipropionic acid.

Mention may be made of the cocoamphodiacetate sold, for example, under the trade name Miranol® C2M concentrate by the company Rhodia Chimie.

(iv) Cationic Surfactant(s):

The lifting composition and/or the color base composition and/or the developer composition may contain at least one cationic surfactant chosen, for example, from: salts of optionally polyoxyalkylenated primary, secondary and tertiary fatty amines; quaternary ammonium salts such as tetra alkyl ammonium, alkylamidoalkyltrialkyl ammonium, trialkylbenzyl ammonium, trialkylhydroxyalkyl ammonium and alkylpyridinium chlorides and bromides; imidazoline derivatives; and cationic amine oxides.

The at least one surfactant may be present in the lifting composition and/or the color base composition and/or the developer composition, in an amount ranging from 0.01% to 40% by weight, such as from 0.05% to 30% by weight, relative to the total weight of each composition.

E. Chelating Agents

The lifting composition and/or the color base composition and/or the developer composition of the present invention may also contain at least one chelating agent. Preferred ranges of chelating agent are from 0.001% to 5% by weight, preferably from 0.005% to 4% by weight, more preferably from 0.01 to 3% by weight of each composition. Preferred chelating agents are EDTA, HEDTA, and sodium or potassium salts, and mixtures, thereof.

F. Antioxidants and Reducing Agents

The lifting composition and/or the color base composition and/or the developer composition of the present invention may also contain at least one antioxidant and/or reducing agent such as ascorbic acid, ascorbylated compounds, such as ascorbyl dipalmitate, t-butylhydroquinone, polyphenols, such as phloroglucinol, thiols, for example, cysteine, sodium sulfite, and sodium hydrosulfite, erythorbic acid, flavonoids, and mixtures thereof. Other examples of reducing agents that are useful include, but are not limited to: anhydrous sodium thiosulfate, powdered sodium metabisulfite, thiourea, ammonium sulfite, thioglycolic acid, thiolactic acid, ammonium thiolactate, glyceryl monothioglycolate, ammonium thioglycolate, thioglycerol, 2,5-dihydroxybenzoic acid, diammonium dithioglycolate, strontium thioglycolate, calcium thiolgycolate, zinc formosulfoxylate, isooctyl thioglycolate, and monoethanolamine thiogylcolate.

The antioxidant and/or reducing agent may be present in the lifting composition and/or the color base composition and/or the developer composition in an amount ranging from 0.1% to 20% by weight relative to the total weight of each composition.

G. Other Ingredients

The compositions of the present invention can also comprise any additive typically used in cosmetic or hair treatment compositions. The additives may include waxes, organogelators, dispersants, oils, preserving agents, fragrances, fillers, neutralizing agents, hydroxy acids, UV filters, ceramides, pseudoceramides, vegetable, mineral oils, synthetic oils, vitamins, and provitamins.

Needless to say, a person skilled in the art will take care to select the optional additional compound(s) mentioned above such that the advantageous properties intrinsically associated with the compositions of the present invention disclosed herein are not, or are not substantially, adversely affected by the envisaged addition(s).

The present invention relates to a method of coloring hair involving applying the lifting composition to the hair, rinsing off the lifting composition from the hair, applying the color base composition, followed by the application of the developer composition onto the hair, at any time thereafter that is convenient to the consumer from the time of application of the color base composition. According to a preferred embodiment, the developer composition is applied up to 60 minutes after application of the color base composition. The hair being colored may be dry, damp or wet.

The lifting composition is applied onto dry, damp or wet hair. The lifting composition, once applied, may then be left on the hair for a period of time sufficient to lighten the hair color to the desired level. The lifting composition is then thoroughly rinsed off from the hair before the color base composition is applied onto the hair.

It should be noted that in between application of the color base composition and the developer composition, the hair is rinsed in order to remove excess color base composition from the hair. The advantage of employing the rinsing step is that the oxidizing agent is then able to react more thoroughly with the oxidation dye precursor present in and around the hair shaft, thereby achieving enhanced fade resistance and less color loss properties.

Thus, the color base composition is rinsed off from the hair before the application of the developer composition.

Moreover, the oxidation dye precursors in the color composition are, in general, colorless or weakly colored. When a rinsing step is employed in between application of the color base and developer compositions, the excess oxidation dye precursors are rinsed from the hair and scalp before application of the developer composition. This then allows the hair color to be formed only between the oxidation dye precursors that remain in and on the hair fibers and the oxidizing agent, thereby minimizing, and perhaps even eliminating, the problems of scalp staining and messy applications encountered with conventional hair dyes systems.

The developer composition, once applied, may then be left on the hair for a period of time ranging from about 1 to about 20 minutes, such as from about 1 to about 10 minutes, and from about 1 to about 5 minutes, in order to develop the intended color/shade within and around the hair shaft. The colored hair is then thoroughly rinsed.

The present invention will be better understood from the examples which follow, all of which are intended for illustrative purposes only, and are not meant to unduly limit the scope of the invention in any way.

EXAMPLES

General procedure: Any lifting composition, including commercial lifting products as described previously, may be used and applied to the hair, according to the product use instructions. After removal of the lifting composition by rinsing the hair the color base composition described hereunder is applied onto individual hair swatches, and allowed to remain in contact therewith. The hair swatches are then rinsed with water. The developer composition described hereunder is then applied onto the hair swatches, and the color is allowed to immediately develop in the hair. The developer composition is allowed to remain in contact with the hair. The hair is then rinsed and dried.

The lifting composition used in the examples hereunder have the following composition:

Lifting Composition: part A Ingredient Wt. % Potassium Persulfate 40.0 Sodium Silicate 23.0 Sodium Persulfate 10.0 Urea 3.0 Acrylates/C10-30 Alkyl Acrylate 3.0 Crosspolymer Magnesium Stearate 2.9 Ammonium Sulfate 2.6 Sodium Metasilicate 2.5 Kaolin 2.3 Sodium Lauryl Sulfate 2.3 Hydrogenated Polydecene 1.7 Magnesium Peroxide 1.5 VP/VA Copolymer 1.0 Magnesium Carbonate 1.0 Guar Gum 0.7 EDTA 0.7 Titanium Dioxide 0.6 Hydroxyethylcellulose 0.5 Sodium Carboxymethyl Starch 0.5 Ultramarines 0.2

Lifting Composition: part B Ingredient Wt. % Water Up to 100% Hydrogen Peroxide 12.0 Cetearyl Alcohol (and) Ceteareth-25 2.85 Trideceth-2 Carboxamide MEA 0.85 Glycerin 0.50 Pentasodium Pentetate 0.15 Sodium Stannate 0.04 Tetrasodium Pyrophosphate 0.02

Just before application onto the hair, the lifting composition was prepared by mixing 1 part by weight of composition A above with 2 parts by weight of composition B above.

Example 1

Color base composition; pH 9.6: Wt. % Ingredient Formula A Hexylene glycol 5 Trideceth-2 carboxamide MEA 1 Cetrimonium chloride 0.008 Aminomethyl propanol 2.37 Potassium sorbate 0.1 Trideceth-6 0.039 Sclerotium gum 0.8 N,N-bis(2-hydroxyethyl)-p- 1 phenylenediamine sulfate 2-oleamido-1,3-octadecanediol 0.01 Propylene glycol 5 2,4-diaminophenoxyethanol HCl 0.8 Isopropyl alcohol 0.18 Amodimethicone 0.46 Behentrimonium chloride 0.79 Sodium metabisulfite 0.7 Erythorbic acid 0.3 Hydroxyethyl cellulose 1 Propylparaben 0.2 Methylparaben 0.2 Water Up to 100

Developer composition Wt. % Ingredient Formula B Potassium persulfate 27.5 Sodium persulfate 10 Silica 2 Sodium metasilicate 2.5 Sodium silicate 7 EDTA 1 Tribehenin 5 Polydecene 45

After removal of the lifting composition, the color base composition is applied onto individual hair swatches, and allowed to remain in contact therewith for approximately 10 minutes. The hair swatches are then rinsed with water. The developer composition is then applied onto the hair swatches, and allowed to remain in contact with the hair for approximately 5 minutes. The hair is then rinsed and dried.

Example 2

This example illustrates another set of color base and developer compositions that may be used and applied to hair previously treated with a lifting composition according to another embodiment of the method of the present invention. In this example, the developer composition is formed by combining 8 parts by weight of the anhydrous oxidizer composition and 92 parts by weight of a shampoo composition described below.

Color Base Composition Ingredients Wt % Deionized Water QS 100% Sodium Hydroxide Adjust to pH = 9.6 Pentasodium Pentetate 2.00 Erythorbic Acid 0.30 Sodium Metabisulfite 0.46 N,N-bis(2-hydroxyethyl)-p-phenylenediamine sulfate 1.00 Cetearyl Alcohol 7.00 2,4-diaminophenoxyethanol HCl 0.80 Fragrance 1.00 Sclerotium Gum 0.80 Chlorhexidine Dihydrochloride 0.05 Methylparaben 0.30 Amodimethicone (and) Trideceth-6 (and) Cetrimonium 1.80 Chloride Propylene Glycol 2.00 Behentrimonium Chloride 4 00 Cocamidopropyl Betaine 10.00 

Oxidizer composition Ingredients Wt % Sodium Persulfate 75.00 Silica 23.30 Polydecene 1.70

Shampoo Composition Ingredients Wt % Ammonium Hydroxide 3.20 Polyquaternium-10 0.80 Disodium Cocoamphodiacetate 10.00 PEG-60 Hydrogenated Castor Oil 0.50 Sodium Laureth Sulfate 13.85 Fragrance, preservatives, UV filters 6.65 Deionized Water QS 100.00%

After removal of the lifting composition, the color base composition described above is applied onto individual hair swatches, and allowed to remain in contact therewith for approximately 10 minutes. The hair swatches are then rinsed with water. The developer composition obtained by mixing the oxidizer composition and the shampoo composition as described above is then applied onto the hair swatches, and allowed to remain in contact with the hair for approximately 5 minutes. The hair is then rinsed and dried. 

1. A method of permanently coloring hair comprising the steps of: (a) applying onto the hair a lifting composition capable of lightening the natural hair color wherein said lifting composition comprises at least one oxidizing agent, chosen from the group formed by hydrogen peroxide, urea peroxide, alkali metal bromates, alkali metal ferricyanides and oxidation-reduction enzymes, optionally in the presence of their respective donor or cofactor; (b) rinsing the lifting composition from the hair, (c) providing a color base composition containing at least one primary dye intermediate chosen from ortho-aminophenols para-aminophenols, ortho-phenylenediamines, para-phenylenediamines, double bases, heterocyclic bases, the acid addition salts thereof, and mixtures thereof; (d) applying the color base composition onto the hair; (e) rinsing the color base composition from the hair; (f) providing a developer composition containing at least one oxidizing agent chosen from persulfates, perborates, percarbonates their salts, and mixtures thereof; and (g) applying the developer composition onto the hair in order to develop color, in situ, in the hair to form colored hair; and (h) rinsing the developer composition from the hair.
 2. The method of claim 1, wherein the color base composition, the lifting composition and the developer composition are substantially free of an oxidation catalyst.
 3. The method of claim 1, wherein the at least one oxidizing agent is chosen from potassium persulfate, sodium persulfate, ammonium persulfate, and mixtures thereof.
 4. The method of claim 1, wherein the at least one oxidizing agent is present in an amount of at least 1% by weight, based on the total weight of the developer composition.
 5. The method of claim 4, wherein the at least one oxidizing agent is present in an amount ranging from 5% to 75% by weight based on the total weight of the developer composition.
 6. The method of claim 5, wherein the at least one oxidizing agent is present in an amount ranging from 6% by weight to 10% by weight based on the total weight of the developer composition.
 7. The method of claim 1, wherein the developer composition does not contain hydrogen peroxide.
 8. The method of claim 1, wherein the pH of the developer composition ranges from 3 to
 11. 9. The method of claim 1, wherein the developer composition is anhydrous.
 10. The method of claim 1, wherein the developer composition comprises at least one solvent chosen from water, organic solvents, and mixtures thereof.
 11. The method of claim 1, wherein the developer composition further comprises a shampoo composition comprising at least one surfactant chosen from anionic, amphoteric, nonionic, zwitterionic, cationic surfactants, and mixtures thereof.
 12. The method of claim 1, wherein the color base composition has a pH ranging from 2 to 6.9.
 13. The method of claim 1, wherein the color base composition has a pH ranging from 7 to
 12. 14. The method of claim 1, wherein the lifting composition is an aqueous solution comprising hydrogen peroxide.
 15. A kit for coloring a keratinous substrate comprising: (a) a multi-unit receptacle; (b) at least one unit comprising a lifting composition capable of lightening the natural hair color wherein said lifting composition comprises at least one oxidizing agent, chosen from the group formed by hydrogen peroxide, urea peroxide, alkali metal bromates, alkali metal ferricyanides and oxidation-reduction enzymes, optionally in the presence of their respective donor or cofactor; (c) at least one unit comprising a color base composition containing at least one primary dye intermediate chosen from ortho-aminophenols, para-aminophenols ortho-pheny lenediamines para-phenylenediamines, double bases, heterocyclic bases, the acid addition salts thereof, and mixtures thereof; and (d) at least one unit comprising a developer composition containing at least one oxidizing agent chosen from persulfates, perborates, percarbonates, their salts, and mixtures thereof.
 16. The method of claim 1, wherein the at least one oxidizing agent is chosen from potassium persulfate, sodium persulfate, ammonium persulfate, and mixtures thereof.
 17. The method of claim 2, wherein the at least one oxidizing agent is present in an amount of at least 1% by weight, based on the total weight of the developer composition.
 18. The method of claim 2, wherein the developer composition does not contain hydrogen peroxide.
 19. The method of claim 3, wherein the developer composition does not contain hydrogen peroxide. 